K-number	K895779
Device name	MODIFIED PERMCATH TRAY (2ND SUBMISSION)
Applicant	Quinton, Inc.
Product code	CBK
Device class	Class II
Decision date	Dec 7, 1989
Decision	Substantially Equivalent
Regulation	868.5895

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View the full FDA submission: accessdata.fda.gov

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MODIFIED PERMCATH TRAY (2ND SUBMISSION)

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